Rosenfeld R D, Miller J A, Narhi L O, Hawkins N, Katta V, Lauren S, Weiss M A, Arakawa T
Amgen Inc., Thousand Oaks, California 91320, USA.
Arch Biochem Biophys. 1997 Jun 15;342(2):298-305. doi: 10.1006/abbi.1997.9996.
Insulin-like growth factor-I (IGF-I) has three disulfide bonds and refolding of the fully reduced molecule generates varying ratios of correctly (PII) and incorrectly (PI) folded forms via several intermediates. All of the intermediates have the disulfide bond between Cys18 and 61 formed, indicating that formation of this disulfide is the first step in refolding. In order to further understand the refolding pathway, two intermediate froms, PIII with the additional disulfide Cys(6/47) formed and PIIIa with Cys(6/48) formed, were isolated. The oxidation of the remaining Cys48 and 52 in PIII and Cys47 and 52 in PIIIa would lead to PI and PII, respectively; however, air oxidation of these resulted in a rapid reshuffling into other intermediates as well as folding into the fully oxidized forms, and this occurred whether refolding was started with PIII or PIIIa. When oxidation occurred in the presence of an excess of oxidized glutathione, the predominant species generated were various glutathione adducts regardless of the initial intermediate form, indicating that formation of the last disulfide bond is not a favorable process relative to disulfide exchange when excess disulfides from oxidized glutathione are present. Interestingly, if 80 microM copper sulfate, an oxidant, is added to the refolding buffer, PIII resulted in formation of the PI form alone, whereas PIIIa resulted in the PII form alone. It was concluded from these results that the intermediate forms of IGF-1 can rapidly reshuffle between different disulfide structures, and that formation of the last disulfide bond is not as favorable a process as the conversion to other intermediates. The oxidation to form the last disulfide bond in PIII or PIIIa is accelerated and hence the interconversion to other intermediates is kinetically minimized only in the presence of copper sulfate. It appears, therefore, that the two intermediate forms, PIII and PIIIa, are the precursors of the corresponding fully oxidized forms, but their conversions are not energetically a favorable process.
胰岛素样生长因子-I(IGF-I)有三个二硫键,完全还原分子的重折叠通过几个中间体产生正确折叠形式(PII)和错误折叠形式(PI)的不同比例。所有中间体均已形成Cys18和61之间的二硫键,表明该二硫键的形成是重折叠的第一步。为了进一步了解重折叠途径,分离出了两种中间体形式,即形成了额外二硫键Cys(6/47)的PIII和形成了Cys(6/48)的PIIIa。PIII中剩余的Cys48和52以及PIIIa中Cys47和52的氧化分别会导致PI和PII;然而,这些中间体的空气氧化会迅速重排为其他中间体,并折叠成完全氧化的形式,无论重折叠是从PIII还是PIIIa开始,都会发生这种情况。当在过量氧化型谷胱甘肽存在下发生氧化时,无论初始中间体形式如何,产生的主要物种都是各种谷胱甘肽加合物,这表明当存在来自氧化型谷胱甘肽的过量二硫键时,相对于二硫键交换,最后一个二硫键的形成不是一个有利的过程。有趣的是,如果将80微摩尔的氧化剂硫酸铜添加到重折叠缓冲液中,PIII仅导致PI形式的形成,而PIIIa仅导致PII形式的形成。从这些结果可以得出结论,IGF-1的中间形式可以在不同的二硫键结构之间快速重排,并且最后一个二硫键的形成不如转化为其他中间体那样是一个有利的过程。在PIII或PIIIa中形成最后一个二硫键的氧化反应会加速,因此只有在硫酸铜存在下,向其他中间体的相互转化在动力学上才会最小化。因此,看来两种中间形式PIII和PIIIa是相应完全氧化形式的前体,但它们的转化在能量上不是一个有利的过程。